Dynamics of non-structural carbohydrate reserves in pruned <Emphasis Type="Italic">Erythrina poeppigiana</Emphasis> and <Emphasis Type="Italic">Gliricidia sepium</Emphasis> trees

In alley cropping systems, fast growing leguminous trees are pruned to reduce competition with crops for light and to provide organic inputs for crop nutrition. Tree regrowth depends on non-structural carbohydrate reserves in the remaining tree parts. In this study, the dynamics of starch and soluble carbohydrates in roots and stems of completely pruned (all shoots removed), partially pruned (one branch retained on the pruned stump) and unpruned Erythrina poeppigiana (Walp.) O.F. Cook and Gliricidia sepium (Jacq.) Kunth ex Walp. trees were studied under humid tropical conditions in Turrialba, Costa Rica. Measurements on starch and soluble carbohydrates in roots and stems were made at 0, 2, 6 and 12 weeks after pruning during both a “rainy” and a “dry” season. In general, the dynamics of non-structural carbohydrates in roots and stems of pruned E. poeppigiana and G. sepium trees were similar. Starch concentration was highest in unpruned trees and higher in roots than in stems of pruned trees. The effect of pruning intensity was first observed in stems, and starch reserves were more depleted in stems than in roots, an effect more evident during the “dry” season. The critical tree regrowth stage for starch mobilisation was that of vigorous sprout development at six or four weeks after pruning particularly in completely pruned trees. At this time, fine root biomass and length and nodule biomass in pruned trees decreased. Survival of fine roots and nodules was greater in partially pruned than in completely pruned trees. Starch accumulation in roots recommenced at 12 weeks after pruning in G. sepium, and later than 12 weeks after pruning in E. poeppigiana roots. This study showed that E. poeppigiana responded better to pruning regimes than G. sepium. Recovery of trees after pruning is better when trees are partially pruned than when completely pruned.     

Fine root dynamics of shaded cacao plantations in Costa Rica

Root turnover may contribute a significant proportion of recycled nutrients in agroforestry systems and competition between trees and crops for nutrients and water may depend on temporal fine root regrowth patterns. Fine root biomass ( 2 mm) and fine root productivity were measured during one year in plantations of cacao (Theobroma cacao) shaded by Erythrina poeppigiana or Cordia alliodora planted on a deep alluvial soil in Turrialba, Costa Rica. Fine root biomass of approximately 1.0 Mg ha^–1 varied little during the year with maximum values at the beginning of the rainy season of 1.85 Mg ha^–1 in the cacao-C. alliodora system compared to 1.20 Mg ha^–1 for cacao-E. poeppigiana. Fine root productivity of C. alliodora and E. poeppigiana (maximum of 205 and 120 kg ha^–1 4 week^–1, respectively) was greatest at the end of the rainy season, while for cacao it was greatest at the beginning of the rainy season (34–68 kg ha^–1 4 week^–1), which suggests that if nutrient competition occurs between the shade trees and the cacao, it could be minimized by early fertilization during the beginning of the rains immediately after pruning the shade trees. Annual fine root turnover was close to 1.0 in both systems. Assuming that fine root biomass in these mature plantations was constant on an annual basis, nutrient inputs from fine root turnover were estimated as 23–24 (N), 2 (P), 14–16 (K), 7–11 (Ca) and 3–10 (Mg) kg ha^–1 year^–1, representing 6–13% and 3–6% of total nutrient input in organic matter in the C. alliodora and E. poeppigiana systems, respectively.     

Pruning effects on root distribution and nutrient dynamics in an acacia hedgerow planting in northern Kenya

Tree pruning is a common management practice in agroforestry for mulching and reducing competition between the annual and perennial crop. The below-ground effects of pruning, however, are poorly understood. Therefore, nutrient dynamics and root distribution were assessed in hedgerow plantings of Acacia saligna (Labill.) H.L. Wendl. after tree pruning. Pruning to a height of 1.5 m was carried out in March and September 1996. In July and October 1996, the fine root distribution (< 2 mm) and their carbohydrate contents were determined at three distances to the tree row by soil coring. At the same time, foliar nutrient contents were assessed, whereas nutrient leaching was measured continuously. The highest root length density (RLD) was always found in the topsoil (0–0.15 m) directly under the hedgerow (0–0.25 m distance to trees). Pruning diminished the RLD in the acacia plots at all depths and positions. The relative vertical distribution of total roots did not differ between trees with or without pruning, but live root abundance in the subsoil was comparatively lower when trees were pruned than without pruning. In the dry season, the proportion of dead roots of pruned acacias was higher than of unpruned ones, while the fine roots of unpruned trees contained more glucose than those of pruned trees. Pruning effectively reduced root development and may decrease potential below-ground competition with intercropped plants, but the reduction in subsoil roots also increased the danger of nutrient losses by leaching. Leaching losses of such mobile nutrients as NO₃^– were likely to occur especially in the alley between pruned hedgerows and tended to be higher after pruning. The reduced size of the root system of pruned acacias negatively affected their P and Mn nutrition. Pruning also reduced the function of the trees as a safety net against the leaching of nutrients for both NO₃^– and Mn, though not for other studied elements. If nutrient capture is an important aim of an agroforestry system, the concept of alley cropping with pruning should be revised for a more efficient nutrient recycling in the system described here.This revised version was published online in November 2005 with corrections to the Cover Date.     

Nitrogen and fine root length dynamics in a tropical agroforestry system with periodically pruned Erythrina poeppigiana

The effect of pruning all branches (complete pruning) or retaining one branch (partial pruning) on the dynamics of nitrogen cycling in aboveground biomass, nitrogen supplying power of an amended Eutric Cambisol, and fine root length, was studied in an Erythrina poeppigiana (Walp.) O.F. Cook—tomato (Lycopersicon esculentum Mill.) alley cropping practice in Turrialba, Costa Rica during 1999–2000. Over the 1 year pruning cycle, in which trees were completely or partially pruned four times, respective aboveground biomass production was 4.4 Mg or 7 Mg ha⁻¹ (2-year-old trees) and 5.5 Mg or 9 Mg ha⁻¹ (8-year-old trees); N cycled in aboveground biomass was 123 kg or 187 kg ha⁻¹ (2-year-old trees) and 160 kg or 256 kg N ha⁻¹ (8-year-old trees); mean fine root length was 489 or 821 m (2-year-old-trees), 184 or 364 m per tree (8-year-old-trees). Pruning intensity did not significantly affect net N mineralisation and net nitrification rates during the tomato-cropping season. For the tomato crop, pre-plant mean net N mineralisation rate of 2.5 mg N kg⁻¹ soil day⁻¹ was significantly lower than 16.7 or 11.6 mg N kg⁻¹ soil day⁻¹ at the end of vegetative development and flowering, respectively. Mean net nitrification rates of 3.5, and 4.3 mg N kg⁻¹ soil day⁻¹, at pre-plant and end of vegetative development, respectively, were significantly higher than 0.3 mg N kg⁻¹ soil day⁻¹ at end of flowering. In humid tropical low-input agroforestry practices that depend on organic inputs from trees for crop nutrition, retention of a branch on the pruned tree stump appears to be a good alternative to removal of all branches for reducing N losses through higher N cycling in aboveground biomass, and for conserving fine root length for higher N uptake, although it might enhance competition for associated crops.     

Fine root distribution of pruned trees and associated crops in a parkland system in Burkina Faso

Besides aboveground interactions, pruning of trees may also modify their rooting pattern for which a better understanding is needed for the optimisation of agroforestry systems. Thus, variation in fine root (d 2 mm) distribution of pruned trees and crops were assessed during three cropping seasons by sampling soil layers at 10 cm intervals up to 50 cm and at four distances from tree trunk. Three crown pruning treatments (totally-pruning, half-pruning and no-pruning) were applied to karité (Vitellaria paradoxa) and néré (Parkia biglobosa). In 1999, 59% (0.477 cm cm^–3) and 69% (0.447 cm cm^–3) of fine roots for karité and néré respectively occurred in the upper 20 cm with a significant decrease in root length density with soil depth. However, in 2000, totally-pruned trees of néré and karité showed 32% (0.051 cm cm^–3) and 34% (0.078 cm cm^–3) of their density in the upper 20 cm whereas root distribution in 2001 was similar to that of 1999. Thus, pruning to reduce belowground competition for the benefit of associated crops can be recommended in the light of the temporary reduction of root density in crop rooting zone and consequently the increase in crop production.This revised version was published online in November 2005 with corrections to the Cover Date.     

Modelling agroforestry systems of cacao (Theobroma cacao) with laurel (Cordia alliodora) or poro (Erythrina poeppigiana) in Costa Rica

Predictive models were developed for Cordia alliodora branch and Theobroma cacao branch or leaf biomass,based on branch basal areas (r² 0.79) but the model of C. alliodora leaf biomass, although significant, was of very low accuracy (r² = 0.09) due to annual leaf fall. At age 10 years, shade tree stem biomass accounted for 80% of the total above-ground biomass of either tree. However, between the ages of 6 and 10 years, the biomass increment of T. cacao branches (3–4t.ha^–1.a^–1) was similar to that of the shade tree stems. During the same period, the net primary productivity was 35 and 28 t.ha^–1.a^–1, for the Erythrina poepigiana and and C. alliodora systems, respectively.Cocoa production under either of the shade trees C. alliodora or E. poeppigiana was 1000 kg.ha^–1.a^–1 (oven-dry; ages 6–10 yr). During the same period, C. alliodora timber production was 9 m³.ha^–1.a^–1 whilst the leguminous shade tree E. poeppigiana does not produce timber. Litterfall over the same 5 years, including crop and/or shade tree pruning residues, averages 11 and 23 t.ha^–1.a^–1, respectively. The main difference was due to E. poeppigiana pruning residues (10t.ha^–1.a^–1).Soil organic material reserves (0–45 cm) increased over 10 years from 198 to 240 t.ha^–1 in the E. poeppigiana plots and from 168–184 t.ha^–1 in the C. alliodora plots. These values, together with the productivity indices presented, provide evidence that the systems are sustainable.For economic reasons, the use of C. alliodora is recommended under the experimental conditions. however, on less fertile soils without fertilization, the greater biomass and hence nutrient return to the soil surface under E. poeppigiana, might make this the preferable shade tree.     

Tree/crop complementarity in an arid zone runoff agroforestry system in northern Kenya

We tested the hypothesis that shallow-rooted crops and deep-rooted trees will share the available water in a complementary manner, when grown together, in a field trail in the Turkana district of northern Kenya during 1994 to 1996. Such studies have been few in dryland agroforestry. The effects of two different Acacia saligna (Labill.) H. Wendl. tree planting densities (2500 and 833 trees per ha), tree pruning (no pruning vs. pruning) and annual intercrops (no intercrop vs. intercrop) on total biomass production and their interactions were tested. In 1996 Sorghum bicolor (L.) Moench was used during the first vegetation period and Vigna unguiculata (L.) Walp. during the second. We used naturally generated runoff water for irrigation to supplement low rainfall amounts typical for the area. High biomass production (> 13 t ha^–1 over a two year period) was observed irrespective of intercropping of pruned trees or sole tree stands. Although the pruning treatment reduced total tree biomass yields by a quarter, the introduction of annual intercrops after the pruning of trees outweighed this loss. The yields of the intercrops in the pruned tree treatments were similar to their yields when grown as monocrops. The calculation of land equivalent ratios showed overyielding for intercropped, pruned systems. The high values for LER (1.36 at low and 1.47 at high density of trees) indicate that there is complementarity in resource use between the different species.This revised version was published online in November 2005 with corrections to the Cover Date.     

C2H2-reduction byErythrina poeppigiana in a Costa Rican coffee plantation

Acetylene reduction activity by root nodules of the legumeErythrina poeppigiana, growing as shade tree in a Costa Rican coffee plantation, was estimated. The mean activity found was 15.7 nmole C₂H₄ · mg (dry weight)^–1 · h^–1. Root nodules collected at different distances from theErythrina stem showed the same activity per dry weight unit. However, as the biomass of the nodules was highest near the stem, was the acetylene reduction activity (expressed per soil volume) maximal near theErythrina stem and declined with distance.     

Water use efficiency and uptake patterns in a runoff agroforestry system in an arid environment

Water is the most limiting factor for plant production in arid to semiarid regions. In order to overcome this limitation surface runoff water can be used to supplement seasonal rainfall. During 1996 we conducted a runoff irrigated agroforestry field trial in the Turkana district of Northern Kenya. The effects of two different Acacia saligna (Labill.) H. Wendl. tree planting densities (2500 and 833 trees per ha), tree pruning (no pruning vs. pruning) and annual intercrops (no intercrop vs. intercrop: Sorghum bicolor (L.) Moench during the first season and Vigna unguiculata (L.) Walp. during the second season) on water use were investigated. The annual crops were also grown as monocrops. Water consumption ranged from 585 to 840 mm during the first season (only treatments including trees). During the second season, which was shorter and the plants relied solely on stored water in the soil profile, water consumption was less than half of that during the first season. Highest water consumptions were found for non-pruned trees at high density and the lowest were found for the annual crops grown as monocrops. Tree pruning decreased water uptake compared to non-pruned trees but soil moisture depletion pattern showed complementarity in water uptake between pruned trees and annual intercrops. The highest values of water use efficiency for an individual treatment were achieved when the pruned trees at high density were intercropped with sorghum (1.59 kg m^–3) and cowpea (1.21 kg m^–3). Intercropping and high tree density increased water use efficiency in our runoff agroforestry trial. We ascribe the observed improvement in water use efficiency to the reduction of unproductive water loss from the bare soil.This revised version was published online in November 2005 with corrections to the Cover Date.     

Fodder production responses to pruning height and fodder quality of some trees and shrubs in a forest-savanna transition zone in southwestern Nigeria

Seasonal fodder production responses of five shrubs (Centrosema arenarium, Desmodium strigillosum, Desmodium velutinum, Phyllodium pulchellum, and Tadehagi triquetrum)and five trees (Albizia gummifera, Berlinia grandiflora, Albizia niopoides, Bauhinia monandra, and Inga edulis) to pruning heights ranging from 15 to 75 cm were evaluated during the main-wet, minor-wet, and dry seasons of 1993 and 1994 in the forest-savanna transition zone of West Africa. Fodder from the main-wet season was analysed for nitrogen (N) and phosphorus (P), and dry matter degradation characteristics after 6, 12, 24, 48, 72 and 96 h of incubation in rumen-fistulated N'Dama steers. In the minor-wet season, fodder production of all species increased in response to increasing pruning height with the exception of P. pulchellum and A. gummifera. Highest fodder production was attained at a pruning height of 45 cm for the Desmodium species, 50 cm for P. pulchellum, and 75 cm for the rest of the species. Concentrations of N and P varied significantly among the species; for N the ranges were 28.7–38.8 g kg^–1 (shrubs) and 25.3–44.5 g kg^–1 (trees), while for P the ranges were 3.26–7.04 g mg^–1 (shrubs) and 3.58–6.76 g mg^–1 (trees). Dry matter degradation characteristics differed significantly among shrubs and trees; ranges for shrubs were: soluble fraction (a), 128–185; degradable fraction (b), 664–703; potential degradability (PD), 793–857, as g kg^–1; rate of degradation (c), 0.0241–0.0308 as % h^–1 while for trees ranges were: (a), 139–160; (b), 651–826; (PD), 824–970, as g kg^–1; (c), 0.0143–0.0227 as % h^–1. Based on fodder production and quality, C. arenarium, D. strigillosum, D. velutinum, B. monandra, I. edulis, and A. niopoides were the most promising species for the development of animal agroforestry technologies in the west African forest-savanna transition zone and similar environments in the tropics.This revised version was published online in November 2005 with corrections to the Cover Date.     

Biomass allocation and nodulation of Gliricidia sepium under two cut-and-carry forage production regimes

The effects of two pruning regimes on the above-ground biomass allocation and nodulation of Gliricidia sepium (Jacq.) Walp. (Leguminosae: Robinieae) were studied in a cut-and-carry forage production system under humid tropical conditions in Guadeloupe, French Antilles. The grass layer composed of a mixture dominated by Paspalum notatum Flügge (80%) and Digitaria decumbens Stent. The pruning regimes were partial pruning (ca. 50%) every two months and complete pruning every six months. The complete pruning caused an almost complete turnover of N2 fixing nodules. The nodule biomass decreased after the partial pruning, but the turnover was not complete. The nodule to foliage biomass ratio followed the same pattern under both treatments, and the values of the ratio converged towards the end of the experimental period. The maxima of standing nodule biomass were 7.2 and 13.0 kg ha−1 in the partially and completely pruned trees, respectively. The cumulative leaf fodder harvest was higher under partial pruning management, due to smaller litter loss. The branch biomass production was higher under complete pruning management. Grass production was not affected by the pruning pattern of G. sepium. It was concluded that the partial pruning management produces more fodder in the studied association, and the nodulation probably adjusts to the canopy N requirements. The potential N release to soil in the turnover of nodules of G. sepium (max. 0.82 kg ha−1) is negligible compared to the N export in tree and grass fodder harvest, 190 and 215 kg ha−1 in partially and completely pruned plots, respectively. This revised version was published online in June 2006 with corrections to the Cover Date.     

Root growth and carbohydrate responses in bearing citrus trees following partial canopy removal

In August, eight 4-m tall citrus trees were pruned by removing the top third of their canopy. Eight unpruned trees served as controls. Root growth, which was examined nondestructively with minirhizotrons over a four-month period, tended to be less in the pruned than unpruned trees seven days after pruning and this difference was significant (P < 0.05) from 14 to 49 days after pruning. Total reducing and ketone sugars (includes free fructose, sucrose and fructans) in the fine roots were less in pruned than unpruned trees 20 days after pruning, but not thereafter. By 30 days after pruning, at least 20% of the roots of the pruned trees at a soil depth of 9 to 35 cm apparently died. By 63 days after pruning, root length density had recovered to that of the unpruned trees, although starch reserves were 18% less in the fine roots of pruned than unpruned trees at this time. Nine to eleven months after pruning (May to July), total biomass of leaves and fine roots to a depth of 1 m were similar in pruned and unpruned trees. However, fruit biomass harvested in April from pruned trees was only 24% of that in the unpruned trees. In May, nonstructural carbohydrates in the fine and coarse roots of pruned trees were generally greater than in unpruned trees, possibly reflecting previous differences in fruit production.     

Above- and below-ground biomass dynamics in a sole cropping and an alley cropping system withGliricidia sepium in the semi-deciduous rainforest zone of West Africa

A considerable amount of data is available about above-ground biomass production and turnover in tropical agroforestry systems, but quantitative information concerning root turnover is lacking. Above- and below-ground biomass dynamics were studied during one year in an alley cropping system withGliricidia sepium and a sole cropping system, on aPlinthic Lixisol in the semi-deciduous rainforest zone of the Côte d'Ivoire. Field crops were maize and groundnut. Live root mass was higher in agroforestry than in sole cropping during most of the study period. This was partly due to increased crop and weed root development and partly to the presence of the hedgerow roots. Fine root production was higher in the alleys and lower under the hedgerows compared to the sole cropping plots. Considering the whole plot area, root production in agroforestry and sole cropping systems was approximatly similar with 1000–1100 kg ha^–1 (dry matter with 45% C) in 0–50 cm depth; about 55% of this root production occured in the top 10 cm. Potential sources of error of the calculation method are discussed on the basis of the compartment flow model. Above-ground biomass production was 11.1 Mg ha^–1 in sole cropping and 13.6 Mg ha^–1 in alley cropping, of which 4.3 Mg ha^–1 were hedgerow prunings. The input of hedgerow root biomass into the soil was limited by the low root mass ofGliricidia as compared to other tree species, and by the decrease of live root mass of hedgerows and associated perennial weeds during the cropping season, presumably as a result of frequent shoot pruning.     

Modelling agroforestry systems of cacao (Theobroma cacao) with laurel (Cordia alliodora) and poro (Erythrina poeppigiana) in Costa Rica II. Cacao and wood production,litter production and decomposition

During 7 years (1979–1985) cacao harvests (beans and husks) have been recorded for the agroforestry systems ofTheobroma cacao underCordia alliodora andErythrina poeppigiana shade trees. The mean oven dry cacao yields were 626 and 712 kg.ha^–1.a^–1 cocoa beans underC. alliodora andE. poeppigiana respectively. Harvests have gradually increased over the years and the plantation has now reached maturity.Annual extraction of N, P, K, Ca and Mg in fruits, which is relatively small, was calculated on the basis of chemical analyses. The following average values were found (kg.ha^–1.a^–1): At the age of 8 years, theC. alliodora trees have reached 26.7 cm diameter (DBH) and 14.0 m in height. Mean annual growth (from age 5 to 7) is 14.6 m³.ha^–1.a^–1.Natural plant residue production has been measured for 4 years (Nov. 1981–Oct. 1985). UnderE. poeppigiana it has reached a value of 8.91 t.ha^–1.a^–1 and underC. alliodora 7.07 t.ha^–1.a^–1. The shade trees have contributed 57 and 47% respectively. Transference and decomposition rates are high and important in the nutrient cycles.The nutrient content of the litter was analysed and corresponding average yearly transfers were (kg.ha^–1.a^–1): For part I see Vol. 4, No. 3, 1986.Agroforestry Project, CATIE/GTZ (Tropical Agricultural Research and Training Center/Gesselschaft für Technische Zusammenarbeit), Turrialba, Costa Rica     

Growth of graded sweetgum 3 years after root and shoot pruning

Nursery grown 1–0 bareroot sweetgum seedlings were lifted and graded into two diameter classes (12–16 and 4–8 mm) during the dormant season. Large and small grades were top and/or root pruned and then outplanted on two sites in the lower Coastal Plain of the southeastern United States. Seedling shoots were pruned to 50% of tree height, a 5 cm stump, or no pruning. Seedling roots were pruned to a 15 cm length or left unpruned. Site affected survival but not growth. Smaller, top pruned seedlings performed worse on one site, probably due to greater weed competition. Large seedlings increased survival and growth which increased 3 year average plot volumes by 89%. Top pruning stimulated height growth, but reduced diameter growth and decreased third year seedling volumes. Root pruning did not affect seedling growth. Diameter growth may better indicate treatment impact that height, which has been most commonly used in previous studies.     

Effects of oak root pruning in forest nurseries on potential pathogen infections

Despite the general practice of root pruning, little is known about the potential impact of reducing shoot/root systems of oak seedlings in this way on their future susceptibility to pathogens, for example Cylindrocarpon spp., Fusarium spp., Ilyonectria spp., Pythium spp. Phytophthora spp. or Rhizoctonia spp. In this study, root‐pruned and non‐pruned seedlings of Quercus robur grown under controlled conditions were inoculated with aggressive and less‐aggressive pathogens. Results indicated, in contrast to our initial assumption, that pathogens significantly reduced lateral root biomass more in non‐pruned seedlings, the extent of the response depending on the pathogens species. In response to pathogen pressure, pruned seedlings tended to attain a higher dry stem mass fraction, but lower dry leaf mass fraction. Pathogens also suppressed leaf mass in total root dry mass fraction (dry leaf mass/total root dry mass ratio, in g × g^?1) more in pruned than in non‐pruned seedlings. These results suggest differences in growth between non‐pruned and pruned seedlings in response to pathogen stress. In nurseries, root pruning of oak trees may enhance the reduction in leaf mass in lateral roots mass fraction resulting from pathogen infections, which may decrease seedling quality. It is therefore important to ensure a low level of inoculum of soil‐borne pathogens to minimize the risk of seedling infection.     

Alley cropping on an Ultisol in subhumid Benin. Part 2: Changes in crop physiology and tree crop competition

From 1986–92 alley cropping with Leucaena leucocephala (Lam.) de Wit and Cajanus cajan (L.) Millsp. was compared to a no-tree control, and fertilisation with 90, 39 and 75 kg ha^–1 N, P and K vs. no fertilisation were studied in maize and cassava grown intercropped or in rotation. Light transmission measurements and row position effects on food crop yield did not indicate any decisive shading effect in tree-crop competition when trees were pruned 2–3 times a year. In the last three years, with NPK in solecropping the crop growth rates (CGR) of maize reached a peak of 100 g m^–1 wk^–1 around 70 days after planting (DAP). CGR in unfertilised Cajanus alleys was as high as in corresponding fertilised treatments but delayed by one month. For cassava, the highest growth rates of 60–130 g m^–1 wk^–1 lasted from 60 to 190 DAP with NPK in solecropping. The harvest index (HI) of cassaca reached 40–50% in all intercropping and unfertilised solecropping treatments. The HI in solecropping was reduced by fertilisation to 30–40% due to excessive leaf growth at 60–190 DAP. The increase in number of thickened roots starting at 30 DAP in solecropping was delayed by one month in intercropping. The reason for significantly higher cassava root yields in Cajanus alleys as compared to no trees in the fertilised solecrop was attributed to the enhanced root formation at 85 DAP due to a slower release of nutrients subject to leaching such as N and K from tree prunings than from mineral fertiliser.     

Biomass production and root distribution of Gmelina arborea under an agrisilviculture system in subhumid tropics of Central India

A study of an agrisilviculture system comprising Gmelina arborea and soybean (Glycine max) was conducted in the subhumid region of Central India. Above- and below-ground biomass production and distribution of coarse and fine roots were studied in 4-year-old G. arborea, planted at a spacing of 2 × 2 m, 2 × 3 m, 2 × 4 m and 2 × 5 m. The total biomass varied from 10.89 Mg ha^–1 to 3.65 Mg ha^–1 depending on the tree density. Among the different tree components, stemwood contributed maximum biomass (54.3–79.4%), followed by branches and leaves. Root distribution pattern showed that most of the coarse roots were distributed in the top 40 cm of soil, whereas fine roots were concentrated in the top 20 cm. Coarse root biomass decreased with an increase in spacing. The spread of roots was asymmetrical in trees planted at 2 × 2 m and 2 × 3 m spacings, while it was symmetrical in trees planted at wide spacings. No significant difference was observed in the fine root biomass in different stands. The root:shoot ratio increased with an increase in spacing. Crop (soybean) growth and productivity varied significantly and it increased with a decrease in tree density. Soybean yield varied between 1.5 Mg ha^–1 to 2.1 Mg ha^–1. The role of root architecture of G. arborea trees on productivity of crops under agri-silviculture system is discussed.     

Litter production and nutrient cycling in coffee (Coffea arabica) or cacao (Theobroma cacao) plantations with shade trees

The relative importance of N fixation, organic material inputs and nutrient inputs in litterfall, as justifications for including shade trees in plantations of coffee or cacao, is discussed. According to existing data, N fixation by leguminous shade trees does not exceed 60 kg.N/ha/a. However, these trees contribute 5,000–10,000 kg. organic material/ha/a.Comparisons are made between the leguminous shade tree Erythrina poeppigiana and the non-leguminous timber tree Cordia alliodora. The former, when pruned 2 or 3 times/a., can return to the litter layer the same amount of nutrients that are applied to coffee plantations via inorganic fertilizers, even at the highest recommended rates for Costa Rica of 270 kg.N, 60 kg.P, 150 kg.K/ha/a. The annual nutrient return in this litterfall represents 90–100 percent of the nutrient store in above-ground biomass of E. poeppigiana, and hence the consequences of competition with the crop should not be a serious limitation. In the case of C. alliodora, which is not pruned, nutrient storage in the tree stems, especially of K, is a potential limiting factor to both crop and tree productivity.It is concluded that, in fertilized plantations of cacao and coffee, litter productivity is a more important shade tree characteristic than N fixation.An early version of this review was presented at the CATIE-IUFRO meeting Los Arboles de Uso Multiple en Sistemas Agroforestales, June 1985, Turrialba, Costa Rica.     

To prune or not to prune Faidherbia albida: competing needs for water,wheat and tree products in semi-arid Ethiopia

Faidherbia albida is one of the scattered trees commonly intercropped with most cereals in Ethiopia due to its positive impacts. The tree is pruned for various purposes including for fencing and fuelwood. In this study, the impact of pruning on water relations of F. albida and on understorey wheat productivity was investigated. The on-farm study was conducted in Ejerssa Joro, semi-arid Ethiopia. Six mature trees were selected; three were fully pruned and three were left unpruned. Sap flow and leaf water potential were measured on these trees. Crop gas exchange, aboveground biomass and grain yield were measured under and outside tree canopies. The highest and the lowest sap volumes, recorded from unpruned F. albida, during the dry period, were 153 L day^?1 and 20 L day^?1, respectively. The highest and the lowest sap volumes were 13.4 L day^?1 and 0.04 L day^?1 recorded during the wet period. Wheat CO₂ assimilation was highest (7.8 µmolm^?2 s^?1) at 1 m distance and declined away from the tree trunk under unpruned trees. Aboveground biomass and grain yield under unpruned treatments were significantly (P?<?0.05) higher than outside of canopy of same tree and outside canopies of pruned trees. Pruning reduced aboveground biomass and grain yield by 30% and 27%, respectively; despite the higher water uptake by unpruned trees. We recommend that intensive pruning of F. albida be discouraged and propose further studies on optimal pruning for increased food production and provision of tree products to meet farmers’ needs.